Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Роль описана достаточно четко и дает возможность работать со специализированными базами клинических исследований в CRO, но зарплата не указана, поэтому сравнить предложение с высоким рыночным ориентиром не получится.
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Зарплата не указанаУзкая специализацияАктуальные инструментыУдалённо по странеОпыт в клинических исследованиях
Оценка от Hirify AI
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Senior Clinical Database Developer (Rave) (Clinical Trials): Developing and maintaining clinical trial databases, data entry screens, edit checks, and integrated EDC systems with an accent on Rave Study Build, Custom Function programming, data quality, and regulatory data standards. Focus on executing UAT, resolving data management issues, supporting database locks and audits, and ensuring the quality and integrity of clinical database deliverables.
Location: Home-based in South Africa; listed locations include Bloemfontein, Johannesburg, Pretoria, Cape Town, and Durban.
Company
hirify.global is a data-focused clinical research organization supporting pharmaceutical, biotech, and medical device companies with clinical trial data management and regulatory submission services.
What you will do
Review clinical trial protocols with clients and advise on effective database data capture.
Develop clinical trial databases, data entry screens, dynamics, edit checks, data listings, and data edits across multiple EDC systems.
Support CRF tracking, external data integration, data validation, query resolution, coding, SAE reconciliation, database lock activities, and QC audits.
Plan and execute user acceptance testing for EDC and integrated systems, including test plans and scripts.
Prepare study documentation and training materials, and train sites and users on EDC applications.
Collaborate with cross-functional teams, resolve client and study-processing issues, and review deliverables for quality and compliance.
Requirements
At least 5 years of experience in clinical database programming.
Strong Rave Study Build skills and mandatory expert-level Custom Function programming experience.
Programming ability in SQL, SAS, or another programming language.
Knowledge of clinical database structures, drug development, clinical trials, and pharmaceutical development processes.
Experience in the pharmaceutical or CRO industry.
Knowledge of CDISC/CDASH standards and their application to CRF and database design; a computer science or related degree is preferred.
Culture & Benefits
Home-based work within South Africa.
Collaborative and inclusive environment within a global clinical research organization.
Opportunity to work on complex clinical trial data and regulatory submission challenges.
Employment with a Great Place to Work certified organization.
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